Barratt BJ - Search Results

1

Evaluation of single nucleotide polymorphism typing with invader on PCR amplicons and its automation.

Mein CA, Barratt BJ, Dunn MG, Siegmund T, Smith AN, Esposito L, Nutland S, Stevens HE, Wilson AJ, Phillips MS, Jarvis N, Law S, de Arruda M, Todd JA. Mein CA, et al. Among authors: barratt bj. Genome Res. 2000 Mar;10(3):330-43. doi: 10.1101/gr.10.3.330. Genome Res. 2000. PMID: 10720574 Free PMC article.

2

Haplotype tag single nucleotide polymorphism analysis of the human orthologues of the rat type 1 diabetes genes Ian4 (Lyp/Iddm1) and Cblb.

Payne F, Smyth DJ, Pask R, Barratt BJ, Cooper JD, Twells RC, Walker NM, Lam AC, Smink LJ, Nutland S, Rance HE, Todd JA. Payne F, et al. Among authors: barratt bj. Diabetes. 2004 Feb;53(2):505-9. doi: 10.2337/diabetes.53.2.505. Diabetes. 2004. PMID: 14747305

3

Investigating the utility of combining phi29 whole genome amplification and highly multiplexed single nucleotide polymorphism BeadArray genotyping.

Pask R, Rance HE, Barratt BJ, Nutland S, Smyth DJ, Sebastian M, Twells RC, Smith A, Lam AC, Smink LJ, Walker NM, Todd JA. Pask R, et al. Among authors: barratt bj. BMC Biotechnol. 2004 Jul 27;4:15. doi: 10.1186/1472-6750-4-15. BMC Biotechnol. 2004. PMID: 15279678 Free PMC article.

4

Genome-wide association studies: theoretical and practical concerns.

Wang WY, Barratt BJ, Clayton DG, Todd JA. Wang WY, et al. Among authors: barratt bj. Nat Rev Genet. 2005 Feb;6(2):109-18. doi: 10.1038/nrg1522. Nat Rev Genet. 2005. PMID: 15716907 Review.

5

Haplotype tagging for the identification of common disease genes.

Johnson GC, Esposito L, Barratt BJ, Smith AN, Heward J, Di Genova G, Ueda H, Cordell HJ, Eaves IA, Dudbridge F, Twells RC, Payne F, Hughes W, Nutland S, Stevens H, Carr P, Tuomilehto-Wolf E, Tuomilehto J, Gough SC, Clayton DG, Todd JA. Johnson GC, et al. Among authors: barratt bj. Nat Genet. 2001 Oct;29(2):233-7. doi: 10.1038/ng1001-233. Nat Genet. 2001. PMID: 11586306

6

Identification of the sources of error in allele frequency estimations from pooled DNA indicates an optimal experimental design.

Barratt BJ, Payne F, Rance HE, Nutland S, Todd JA, Clayton DG. Barratt BJ, et al. Ann Hum Genet. 2002 Nov;66(Pt 5-6):393-405. doi: 10.1017/S0003480002001252. Ann Hum Genet. 2002. PMID: 12485472

7

Lack of association of the Ala(45)Thr polymorphism and other common variants of the NeuroD gene with type 1 diabetes.

Vella A, Howson JM, Barratt BJ, Twells RC, Rance HE, Nutland S, Tuomilehto-Wolf E, Tuomilehto J, Undlien DE, Rønningen KS, Guja C, Ionescu-Tîrgovişte C, Savage DA, Todd JA. Vella A, et al. Among authors: barratt bj. Diabetes. 2004 Apr;53(4):1158-61. doi: 10.2337/diabetes.53.4.1158. Diabetes. 2004. PMID: 15047635

8

Development of an integrated genome informatics, data management and workflow infrastructure: a toolbox for the study of complex disease genetics.

Burren OS, Healy BC, Lam AC, Schuilenburg H, Dolman GE, Everett VH, Laneri D, Nutland S, Rance HE, Payne F, Smyth D, Lowe C, Barratt BJ, Twells RC, Rainbow DB, Wicker LS, Todd JA, Walker NM, Smink LJ. Burren OS, et al. Among authors: barratt bj. Hum Genomics. 2004 Jan;1(2):98-109. doi: 10.1186/1479-7364-1-2-98. Hum Genomics. 2004. PMID: 15601538 Free PMC article.

9

Comparison of population- and family-based methods for genetic association analysis in the presence of interacting loci.

Howson JM, Barratt BJ, Todd JA, Cordell HJ. Howson JM, et al. Among authors: barratt bj. Genet Epidemiol. 2005 Jul;29(1):51-67. doi: 10.1002/gepi.20077. Genet Epidemiol. 2005. PMID: 15892093

10

Sequencing and association analysis of the type 1 diabetes-linked region on chromosome 10p12-q11.

Nejentsev S, Smink LJ, Smyth D, Bailey R, Lowe CE, Payne F, Masters J, Godfrey L, Lam A, Burren O, Stevens H, Nutland S, Walker NM, Smith A, Twells R, Barratt BJ, Wright C, French L, Chen Y, Deloukas P, Rogers J, Dunham I, Todd JA. Nejentsev S, et al. Among authors: barratt bj. BMC Genet. 2007 May 17;8:24. doi: 10.1186/1471-2156-8-24. BMC Genet. 2007. PMID: 17509149 Free PMC article.

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